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Quoted phrase not found in phrase index: "Retinitis pigmentosa 40"
Page 1
Retinitis pigmentosa.
Hamel C. Hamel C. Orphanet J Rare Dis. 2006 Oct 11;1:40. doi: 10.1186/1750-1172-1-40. Orphanet J Rare Dis. 2006. PMID: 17032466 Free PMC article. Review.
Retinitis pigmentosa (RP) is an inherited retinal dystrophy caused by the loss of photoreceptors and characterized by retinal pigment deposits visible on fundus examination. ...Currently, there is no therapy that stops the evolution of the disease or restores the vi …
Retinitis pigmentosa (RP) is an inherited retinal dystrophy caused by the loss of photoreceptors and characterized by retinal …
Driving with retinitis pigmentosa.
Heath Jeffery RC, Lo J, Thompson JA, Lamey TM, McLaren TL, DeRoach JN, Kabilio MS, Chen FK. Heath Jeffery RC, et al. Ophthalmic Genet. 2023 Aug;44(4):352-360. doi: 10.1080/13816810.2023.2196338. Epub 2023 Apr 4. Ophthalmic Genet. 2023. PMID: 37013444
BACKGROUND: To establish the proportion of patients with retinitis pigmentosa (RP) meeting the Australian fitness to drive (FTD) visual standards. ...BEVF testing is essential in the assessment of RP patients who are still driving. Phenotype and genotype predicto …
BACKGROUND: To establish the proportion of patients with retinitis pigmentosa (RP) meeting the Australian fitness to drive (FT …
Cone rod dystrophies.
Hamel CP. Hamel CP. Orphanet J Rare Dis. 2007 Feb 1;2:7. doi: 10.1186/1750-1172-2-7. Orphanet J Rare Dis. 2007. PMID: 17270046 Free PMC article. Review.
CRDs are characterized by retinal pigment deposits visible on fundus examination, predominantly localized to the macular region. In contrast to typical retinitis pigmentosa (RP), also called the rod cone dystrophies (RCDs) resulting from the primary loss in rod phot …
CRDs are characterized by retinal pigment deposits visible on fundus examination, predominantly localized to the macular region. In contrast …
Next-generation sequencing and its application in diagnosis of retinitis pigmentosa.
Salmaninejad A, Motaee J, Farjami M, Alimardani M, Esmaeilie A, Pasdar A. Salmaninejad A, et al. Ophthalmic Genet. 2019 Oct;40(5):393-402. doi: 10.1080/13816810.2019.1675178. Ophthalmic Genet. 2019. PMID: 31755340 Review.
Retinitis Pigmentosa (RP) is a major cause of heritable human blindness with a high genetic heterogeneity. ...A precise molecular diagnosis is crucial for disease characterization and clinical prognosis. DNA sequencing is a powerful tool for deciphering vario …
Retinitis Pigmentosa (RP) is a major cause of heritable human blindness with a high genetic heterogeneity. ...A precise molecu …
Genetic markers for retinitis pigmentosa.
Wang DY, Chan WM, Tam PO, Chiang SW, Lam DS, Chong KK, Pang CP. Wang DY, et al. Hong Kong Med J. 2005 Aug;11(4):281-8. Hong Kong Med J. 2005. PMID: 16085945 Free article. Review.
OBJECTIVE: To review recent advances in the molecular genetics of retinitis pigmentosa with emphasis on the development of genetic markers that aids diagnosis and prognosis. ...A large number of mutations are known to cause retinitis pigmentosa. …
OBJECTIVE: To review recent advances in the molecular genetics of retinitis pigmentosa with emphasis on the development of gen …
Prediction of visual impairment in retinitis pigmentosa using deep learning and multimodal fundus images.
Liu TYA, Ling C, Hahn L, Jones CK, Boon CJ, Singh MS. Liu TYA, et al. Br J Ophthalmol. 2023 Oct;107(10):1484-1489. doi: 10.1136/bjo-2021-320897. Epub 2022 Jul 27. Br J Ophthalmol. 2023. PMID: 35896367 Free PMC article.
BACKGROUND: The efficiency of clinical trials for retinitis pigmentosa (RP) treatment is limited by the screening burden and lack of reliable surrogate markers for functional end points. ...In external testing (AUMC dataset, 349 images, 166 eyes, 83 patients), the A …
BACKGROUND: The efficiency of clinical trials for retinitis pigmentosa (RP) treatment is limited by the screening burden and l …
Nutrition and retinal degenerations.
Berson EL. Berson EL. Int Ophthalmol Clin. 2000 Fall;40(4):93-111. doi: 10.1097/00004397-200010000-00008. Int Ophthalmol Clin. 2000. PMID: 11064860 Review.
Nutritional approaches to treatment have proved successful in the case of the common forms of retinitis pigmentosa (supplementation with vitamin A), Bassen-Kornzweig disease (supplementation with vitamins A, E, and K), gyrate atrophy (low-protein, low-arginine diet …
Nutritional approaches to treatment have proved successful in the case of the common forms of retinitis pigmentosa (supplement …
Evaluation of the Choroid in Eyes With Retinitis Pigmentosa and Cystoid Macular Edema.
Iovino C, Au A, Hilely A, Violanti S, Peiretti E, Gorin MB, Sarraf D. Iovino C, et al. Invest Ophthalmol Vis Sci. 2019 Dec 2;60(15):5000-5006. doi: 10.1167/iovs.19-27300. Invest Ophthalmol Vis Sci. 2019. PMID: 31794599
PURPOSE: To study the anatomical choroidal features associated with the presence of cystoid macular edema (CME) in eyes with retinitis pigmentosa (RP). METHODS: A total of 159 eyes (from 159 patients) with a diagnosis of RP were enrolled in this retrospective cross- …
PURPOSE: To study the anatomical choroidal features associated with the presence of cystoid macular edema (CME) in eyes with retinitis …
Prevalence of cystoid macular oedema, epiretinal membrane and cataract in retinitis pigmentosa.
Liew G, Strong S, Bradley P, Severn P, Moore AT, Webster AR, Mitchell P, Kifley A, Michaelides M. Liew G, et al. Br J Ophthalmol. 2019 Aug;103(8):1163-1166. doi: 10.1136/bjophthalmol-2018-311964. Epub 2018 Oct 5. Br J Ophthalmol. 2019. PMID: 30291136
BACKGROUND/AIMS: To report the prevalence of treatable complications (cystoid macular oedema, CME; epiretinal membrane, ERM and cataract) in patients with retinitis pigmentosa (RP). METHODS: Consecutive patients with RP attending a tertiary eye clinic in 2012. ...
BACKGROUND/AIMS: To report the prevalence of treatable complications (cystoid macular oedema, CME; epiretinal membrane, ERM and cataract) in …
Genotypes and clinical features of RHO-associated retinitis pigmentosa in a Japanese population.
Tsutsui S, Murakami Y, Fujiwara K, Koyanagi Y, Akiyama M, Takeda A, Ikeda Y, Sonoda KH. Tsutsui S, et al. Jpn J Ophthalmol. 2024 Jan;68(1):1-11. doi: 10.1007/s10384-023-01036-0. Epub 2023 Dec 9. Jpn J Ophthalmol. 2024. PMID: 38070066
PURPOSE: To report the genotypes and clinical features of RHO-associated retinitis pigmentosa (RHO-RP) in the Kyushu region of Japan. STUDY DESIGN: Retrospective, single-center study. ...[Pro347Leu] variant showed a more severe phenotype, and variants causing sector …
PURPOSE: To report the genotypes and clinical features of RHO-associated retinitis pigmentosa (RHO-RP) in the Kyushu region of …
128 results